Apply pharmacovigilance expertise remotely with Cencora as a Drug Safety Associate supporting Innomar Strategies in Canada. Review safety data, complaints, and clinical information.

This full-time, six-month contract supports patient and provider services and pharmaceutical commercialization. The role requires adverse event triage, database entry, source data review, and quality checks. You will work with internal and external clients to clarify information and complete documentation.

Key Responsibilities:

- Receive, scan, and document pertinent clinical information
- Review source documents and triage adverse event information
- Enter adverse events and quality complaints into databases
- Perform quality checks and source data verification




- Screen medical literature for safety information

Requirements:

- Minimum college-level education required
- One to three years’ related experience
- Knowledge of pharmacovigilance guidelines and industry practices
- Robust analytical, organizational, and communication skills
- Microsoft Office skills and reliable internet for remote work

Use analytical, detail-focused pharmacovigilance skills to support Cencora’s remote Drug Safety Associate contract.

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📌 Remote Drug Safety Associate (Moncton)
🏢 Cencora
📍 Moncton